Ding Bingjie, Li Mengjuan, Liu Liu, Song Xuewen, Zhang Yuanyuan, Xia Ao, Liu Jingyuan, Zhou Hu
Department of Hematology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Hemostasis and Thrombosis Diagnostic Engineering Research Center of Henan Province, Zhengzhou, China.
Department of Hematology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Cancer Rep (Hoboken). 2025 Feb;8(2):e70152. doi: 10.1002/cnr2.70152.
Immune thrombocytopenia (ITP) is an acquired autoimmune disease characterised by low platelet count. Treatment discontinuation or heterogeneity in the pathogenesis of ITP heightens the occurrence of relapsed or refractory ITP. Bruton's tyrosine kinase (BTK) has emerged as a promising target for autoimmune disorders.
In this case series, we have explored the efficacy and safety of Bruton's tyrosine kinase inhibitors (BTKi) in treating relapsed/refractory ITP, by retrospective analysis of the diagnostic history and efficacy of four patients with relapsed/refractory ITP who attended the Affiliated Cancer Hospital of Zhengzhou University and were treated with BTKi. All four patients received > 4 lines of ITP treatment and did not respond to splenectomy or other interventions before and after treatment with BTK inhibitor. After adjusting to the treatment with BTKi, one patient achieved a complete response, and two patients achieved a partial response. All three patients achieved sustained remission with platelet counts of > 50 × 10/L maintained for 1045, 390 and 334 days, respectively. Another patient died of intracranial haemorrhage due to a decline in the platelet count after discontinuation of the drug, and the duration of sustained remission before discontinuation of the drug was 120 days. Four patients had no significant abnormalities in the functions of the liver and kidney monitored during the treatment period.
For patients with relapsed/refractory ITP, BTK inhibitor therapy can be considered as an option, with promising preliminary efficacy and safety. However, more clinical trials are needed to verify the exact data.
免疫性血小板减少症(ITP)是一种以血小板计数低为特征的获得性自身免疫性疾病。ITP发病机制中的治疗中断或异质性增加了复发或难治性ITP的发生。布鲁顿酪氨酸激酶(BTK)已成为自身免疫性疾病的一个有前景的靶点。
在本病例系列中,我们通过回顾性分析郑州大学附属肿瘤医院4例接受BTK抑制剂治疗的复发/难治性ITP患者的诊断病史和疗效,探讨了布鲁顿酪氨酸激酶抑制剂(BTKi)治疗复发/难治性ITP的疗效和安全性。所有4例患者均接受了>4线的ITP治疗,在接受BTK抑制剂治疗前后对脾切除术或其他干预措施均无反应。调整为BTKi治疗后,1例患者获得完全缓解,2例患者获得部分缓解。所有3例患者均实现持续缓解,血小板计数分别维持在>50×10⁹/L达1045、390和334天。另1例患者在停药后因血小板计数下降死于颅内出血,停药前持续缓解时间为120天。4例患者在治疗期间监测的肝肾功能无明显异常。
对于复发/难治性ITP患者,BTK抑制剂治疗可作为一种选择,初步疗效和安全性良好。然而,需要更多的临床试验来验证确切数据。